Literature DB >> 32925194

Claudin-18 as a Marker for Identifying the Stomach and Pancreatobiliary Tract as the Primary Sites of Metastatic Adenocarcinoma.

Wan-Ting Li1, Yung-Ming Jeng1, Ching-Yao Yang2.   

Abstract

Identification of the primary site of cancer is essential for the treatment of patients with cancer. Numerous immunohistochemical markers have been developed to determine the differentiation of tumor cells and suggest possible primary sites, but markers of gastric and pancreatic adenocarcinomas are still lacking. Claudin-18 is a tight-junction protein uniquely expressed in gastric epithelial cells and has been shown to be expressed in gastric and pancreatic adenocarcinoma. Whether claudin-18 can be used as a marker for identifying the primary site of cancer is still unclear. In this study, we used the immunohistochemical method to stain claudin-18 in tissue arrays containing 575 carcinomas from different anatomic sites and representative sections of 157 metastatic adenocarcinomas. In the group of primary tumors, claudin-18 was frequently expressed in gastric, pancreatic, and pulmonary mucinous adenocarcinomas. Half of cholangiocarcinomas and ovarian mucinous carcinomas and some colorectal and pulmonary adenocarcinomas were also positive for claudin-18. In the metastatic cohort, 15 of 17 (88%) gastric adenocarcinomas, 18 of 23 (78%) pancreatic adenocarcinomas, and 4 of 7 (57%) cholangiocarcinomas and gallbladder adenocarcinomas were positive for claudin-18. Only 4 tumors that originated outside the stomach and pancreatobiliary tract were positive for claudin-18. After normalization to the tumor frequency, the sensitivity of claudin-18 for identifying the stomach and pancreatobiliary tract as primary tumor sites was 79%, and the specificity was 93%. The positive and negative predictive values were 76% and 94%, respectively. In conclusion, claudin-18 represents a sensitive and specific marker for stomach and pancreatobiliary adenocarcinoma that may be a useful diagnostic tool in routine surgical pathology.

Entities:  

Year:  2020        PMID: 32925194     DOI: 10.1097/PAS.0000000000001583

Source DB:  PubMed          Journal:  Am J Surg Pathol        ISSN: 0147-5185            Impact factor:   6.394


  5 in total

1.  Decreased expression of claudin-18.2 in alpha-fetoprotein-producing gastric cancer compared to conventional gastric cancer.

Authors:  Weiwei Weng; Meng Zhang; Shujuan Ni; Cong Tan; Midie Xu; Xin Wang; Hui Sun; Lei Wang; Dan Huang; Weiqi Sheng
Journal:  J Gastrointest Oncol       Date:  2022-06

2.  Claudin-18 as a Promising Surrogate Marker for Endocervical Gastric-type Carcinoma.

Authors:  Takako Kiyokawa; Lien Hoang; Anna Pesci; Isabel Alvarado-Cabrero; Esther Oliva; Kay J Park; Robert A Soslow; Simona Stolnicu
Journal:  Am J Surg Pathol       Date:  2022-05-01       Impact factor: 6.298

3.  Claudin 18.2 is a potential therapeutic target for zolbetuximab in pancreatic ductal adenocarcinoma.

Authors:  Xi Wang; Cheng-Sheng Zhang; Xu-Yuan Dong; Yuan Hu; Bao-Jun Duan; Jun Bai; Yin-Ying Wu; Lin Fan; Xin-Hua Liao; Ye Kang; Peng Zhang; Meng-Yang Li; Jiao Xu; Zhi-Jun Mao; Hui-Tong Liu; Xiao-Long Zhang; Li-Fei Tian; En-Xiao Li
Journal:  World J Gastrointest Oncol       Date:  2022-07-15

Review 4.  Claudins and Gastric Cancer: An Overview.

Authors:  Itaru Hashimoto; Takashi Oshima
Journal:  Cancers (Basel)       Date:  2022-01-07       Impact factor: 6.639

Review 5.  Gastric Cancer: Mechanisms, Biomarkers, and Therapeutic Approaches.

Authors:  Sangjoon Choi; Sujin Park; Hyunjin Kim; So Young Kang; Soomin Ahn; Kyoung-Mee Kim
Journal:  Biomedicines       Date:  2022-02-24
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.